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Fully Automated Production of Diverse 18F-Labeled PET Tracers on the ELIXYS Multireactor Radiosynthesizer Without Hardware Modification.

Authors :
Lazari, Mark
Collins, Jeffrey
Shen, Bin
Farhoud, Mohammed
Yen, Daniel
Maraglia, Brandon
Chin, Frederick T.
Nathanson, David A.
Moore, Melissa
van Dam, R. Michael
Source :
Journal of Nuclear Medicine Technology; Sep2014, Vol. 42 Issue 3, p203-210, 8p, 1 Color Photograph, 2 Diagrams, 2 Graphs
Publication Year :
2014

Abstract

Fully automated radiosynthesizers are continuing to be developed to meet the growing need for the reliable production of PET tracers made under current good manufacturing practice guidelines. There is a current trend toward supporting kitlike disposable cassettes that come preconfigured for particular tracers, thus eliminating the need for cleaning protocols between syntheses and enabling quick transitions to synthesizing other tracers. Though ideal for production, these systems are often limited for the development of novel tracers because of pressure, temperature, and chemical compatibility considerations. This study demonstrated the versatile use of the ELIXYS fully automated radiosynthesizer to adapt and produce 8 different <superscript>18</superscript>F-labeled PET tracers of varying complexity. Methods: Three-reactor syntheses of 2-deoxy-2-<superscript>18</superscript>F-fluoro-P-D-arabinofuranosylcytosine (D-<superscript>18</superscript>F-FAC), 2-deoxy-2-<superscript>18</superscript>F-fluoro-5-methyl-p-L-arabinofuranosyluracil (L-<superscript>18</superscript>F-FMAU), and 2-deoxy-2-<superscript>18</superscript>F-fluoro-5-ethyl-p-D-arabinofuranosyluracil (D-<superscript>18</superscript>F-FEAU) along with the 1-reactor syntheses of D-<superscript>18</superscript>F-FEAU, <superscript>18</superscript>F-FDG, 3-deoxy-3-<superscript>18</superscript>F-fluoro-L-thymidine (<superscript>18</superscript>F-FLT), <superscript>18</superscript>F-fallypride, 9-(4-<superscript>18</superscript>F-fluoro-3-hydroxymethylbutyl)-guanine (<superscript>18</superscript>F-FHBG), and N-succinimidyl-4-<superscript>18</superscript>F-fluorobenzoate (<superscript>18</superscript>F-SFB), were all produced using ELIXYS without the need for any hardware modifications or reconfiguration. Synthesis protocols were adapted and slightly modified from those in the literature but were not fully optimized. Furthermore, <superscript>18</superscript>F-FLT, <superscript>18</superscript>F-FDG, and <superscript>18</superscript>F-fallypride were produced sequentially on the same day and used for preclinical imaging of A431 tumor-bearing severe combined immunodeficient mice and wild-type BALB/c mice. To assess future translation to the clinical setting, several batches of tracers were subjected to a full set of quality control tests. Results: All tracers were produced with radiochem-ical yields comparable to those in the literature. <superscript>18</superscript>F-FLT, <superscript>18</superscript>F-FDG, and <superscript>18</superscript>F-fallypride were successfully used to image the mice, with results consistent with those reported in the literature. All tracers that were subjected to clinical quality control tests passed. Conclusion: The ELIXYS radiosynthesizer facilitates rapid tracer development and is capable of producing multiple <superscript>18</superscript>F-labeled PET tracers suitable for clinical applications using the same hardware setup. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00914916
Volume :
42
Issue :
3
Database :
Complementary Index
Journal :
Journal of Nuclear Medicine Technology
Publication Type :
Academic Journal
Accession number :
98167266
Full Text :
https://doi.org/10.2967/jnmt.114.140392